From: Society for Cardiovascular Magnetic Resonance 2020 Case of the Week series
 | Age | Location | CMR features | Remarks |
---|---|---|---|---|
Benign | ||||
 Rhabdomyoma | < 4 years | Intramyocardial or intracavitary; any chamber | Homogeneous on all sequences; no enhancement | Frequent association with tuberous sclerosis |
 Fibroma | Majority < 1 year | Ventricular septum or free wall | Peripheral enhancement; signal void due to calcifications | Associated with Gorlin syndrome |
 Teratoma | Children | Pericardial; Usually left atrium if intramyocardial (rare) | Multiloculated mixed solid cystic mass |  |
 Hemangioma | Any age | Ventricular septum or right atrium; intramural or endocardial | T2 hyperintense with heterogeneous enhancement; hyperintense on perfusion sequence |  |
Malignant | ||||
 Lymphoma | Older children and adolescents | Right atrium and right ventricle more common | Lobulated enhancing mass | Typically non-Hodgkin lymphoma |
 Sarcoma | Young children | Right and left atria more common | Infiltrative irregular mass with heterogeneous enhancement; hemorrhagic pericardial effusion may be present |  |
 Metastasis | Any age | Right heart | Variable features depending on primary tumor |  |
Non-neoplastic | ||||
 Thrombus | Depends on underlying etiology | Commonly left ventricle; Right atrium in the presence of central venous catheter | Variable signal depending on age of thrombus; no enhancement (surface enhancement may be present in chronic organized thrombus) | Commonly associated with indwelling central venous catheters, congenital heart disease and Kawasaki’s disease |